Apoptosis induced by chamaejasmine in human osteosarcoma cells through p53 pathway

Tumour Biol. 2015 Jul;36(7):5433-9. doi: 10.1007/s13277-015-3209-5. Epub 2015 Feb 14.

Abstract

Osteosarcoma cancer is one of the most lethal malignancies, and there is no effective preventive measure to date. Chamaejasmine is the major ingredient in Stellera chamaejasme L. Except its potent pain-relieving efficacy as reported, chamaejasmine also exerted its anti-tumor activity in several tumor models. Here, we reported that chamaejasmine had a profound anti-proliferative effect on human osteosarcoma cells in a concentration-dependent and time-dependent manner, which was associated with an increase of p21 and bax and a decrease of bcl-2 and consequently increased caspase-3 activity. The main mechanism of anti-tumor potency was mainly attributed to the induction of p53. Chamaejasmine hugely elevated the expression of p53. The results of p53 shRNA experiment further demonstrated that p53 knockdown severely impaired the sensitivity of tested cells to chamaejasmine, implicating the important role of p53 played in chamaejasmine's anti-tumor activity. In conclusion, results showed chamaejasmine induced apoptosis in MG63 cells and could be a candidate drug for osteosarcoma cancer chemoprevention.

MeSH terms

  • Apoptosis / drug effects
  • Biflavonoids / administration & dosage*
  • Bone Neoplasms / drug therapy*
  • Bone Neoplasms / genetics
  • Bone Neoplasms / pathology
  • Cell Line, Tumor
  • Humans
  • Osteosarcoma / drug therapy*
  • Osteosarcoma / genetics
  • Osteosarcoma / pathology
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • RNA, Small Interfering / genetics
  • Signal Transduction / drug effects
  • Tumor Suppressor Protein p53 / biosynthesis*
  • Tumor Suppressor Protein p53 / genetics
  • bcl-2-Associated X Protein / biosynthesis
  • p21-Activated Kinases / biosynthesis

Substances

  • Biflavonoids
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Small Interfering
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • chamaejasmine
  • PAK2 protein, human
  • p21-Activated Kinases